NDC 81702-205 Dr. Pelo Scalp Tonic Sheet
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81702 - Jrj.,inc
- 81702-205 - Dr. Pelo Scalp Tonic Sheet
Product Packages
NDC Code 81702-205-01
Package Description: 25 mL in 1 POUCH
Product Details
What is NDC 81702-205?
What are the uses for Dr. Pelo Scalp Tonic Sheet?
Which are Dr. Pelo Scalp Tonic Sheet UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Dr. Pelo Scalp Tonic Sheet Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- COIX LACRYMA-JOBI VAR. MA-YUEN SEED (UNII: 8DW238I7ZI)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- WATER (UNII: 059QF0KO0R)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- REYNOUTRIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- ALCOHOL (UNII: 3K9958V90M)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- ALLANTOIN (UNII: 344S277G0Z)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- HYALURONIC ACID (UNII: S270N0TRQY)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".